FDA MedTech Regulatory Forum – EU MDR Panel

August 22, 2019 — Akron, OH

Moderating and presenting? Nobody who knows R&Q's Executive Director of Regulatory & Quality Consulting Services, Nancy Morrison, is surprised. Nancy will be pulling double duty during for an EU MDR transition session at BioOhio's FDA MedTech Regulatory Forum on Thursday, August 22nd.

Read on for all the details.

What

EU MDR Transition Progress (panel discussion)

Where

Bounce Innovation Hub

526 S. Main St.

Akron, Ohio 44311

When

Thursday, August 22nd: 1:15pm

Who

Holly Lee – Senior Manager, Post-Market Surveillance
Philips Medical

Notified Body (still to be announced)

Nancy Morrison – Executive Director, Regulatory & Quality Consulting Services
Regulatory & Quality Solutions (R&Q)

Nancy has over 25 years of quality and regulatory experience in the medical industry with US and global regulatory submission experience. The previous five years have been with R&Q working with start-up, mid-size and multi-national medical device and combination product companies. Nancy has a Bachelor of Science in Mathematics and an Advanced Certificate in Regulatory Affairs along with RAC certifications for the US and EU. Nancy has the ability to build collaborative relationships with stakeholders to utilize regulations to identify opportunities that provide compliant and effective business solutions.

Check out all the event details and register here.